日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Ontogeny Dictates Oncogenic Potential, Lineage Hierarchy, and Therapy Response in Pediatric Leukemia.

儿童白血病的致癌潜能、谱系等级和治疗反应由个体发育决定。

Wang Ke, Saniei Shayan, Poddar Nikita, Martinez Isabella G, Chao Clifford, Autar Subrina, Fiore Persephone, Carcamo Saul, Sreenath Meghana, Peplinski Jack H, Ries Rhonda E, Mei Anna Huo-Chang, Rahman Noshin Azra, Mekerishvili Levan, Quijada-Álamo Miguel, Freed Grace, Zhang Mimi, Lachman Katherine, Diaz Zayna, Gonzalez Manuel M, Zhang Jing, Pham Giang, Filipescu Dan, Berisa Mirela, Balestra Tommaso, Wheeler Noelle, Reisz Julie A, D'Alessandro Angelo, Puleston Daniel J, Bernstein Emily, Chipuk Jerry E, Wunderlich Mark, Tasian Sarah K, Marcellino Bridget K, Glass Ian A, Sturgeon Christopher M, Landau Dan A, Chen Zhihong, Papapetrou Eirini P, Izzo Franco, Meshinchi Soheil, Hasson Dan, Wagenblast Elvin

Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

非编码RNA基因RNU4-2的双等位基因变异会导致一种隐性遗传的神经发育综合征,并伴有明显的白质改变。

Rius, Rocio; Blakes, Alexander J M; Chen, Yuyang; De Jonghe, Joachim; Lecoquierre, François; Dawes, Ruebena; Cogne, Benjamin; Kim, Hyung Chul; Alvi, Javeria R; Amblard, Florence; Ansari, Morad; Arlt, Annabelle; Austin-Tse, Christina; Baer, Sarah; Balasubramanian, Meena; Balton, Elsa V; Barcia, Giulia; Beleza-Meireles, Ana; Bernstein, Jonathan A; Beygo, Jasmin; Blanc, Pierre; Bramswig, Nuria C; Braun, Frederik; Buchzik, Daniel; Calame, Daniel G; Campbell, Jamie; Coutton, Charles; Cunningham, Chloe A; Dargie, Nitsuh; Depienne, Christel; Dipple, Katrina M; Dieux, Anne; Dixit, Abhijit; Dreyer, Lauren; Du, Haowei; El Chehadeh, Salima; Field, Michael; Ewans, Lisa J; Geiger, Vanessa; Gibbs, Richard A; Glass, Ian; Grunewald, Olivier; Gueguen, Paul; Haack, Tobias B; Hadj Abdallah, Hamza; Harbuz, Radu; Helbig, Ingo; Horvath, Judit; Hustinx, Alexander; Isidor, Bertrand; Jacquemont, Marie-Line; Jamie, Fraser; Jeanne, Médéric; Kessler, Riley; Klinkhammer, Hannah; Korenke, G Christoph; Kotzaeridou, Urania; Krawitz, Peter; Laurie, Steven; Leventer, Richard J; Levy, Rebecca J; Lupski, James R; Marijon, Pierre; McGinnis, Kaitlin E; Mendez, Rodrigo; Messaoud, Olfa; Nava, Caroline; Nizard, Mevyn; O'Donnell-Luria, Anne; O'Leary, Melanie C; Olivieri, Simone; Parida, Amitav; Pehlivan, Davut; Prentice, Anna Jenne; Posey, Jennifer E; Reuter, Chloe M; Satre, Véronique; Schluth-Bolard, Caroline; Smol, Thomas; Sultan, Tipu; Taylor, John; Thauvin-Robinetvin, Christel; Thevenon, Julien; Uebergang, Eloise; Ueberberg, Sandra; Vincent-Delorme, Catherine; Wassmer, Evangeline; Westwood, Emma; Wheeler, Matthew T; Gulec, Elif Yilmaz; Vanderver, Adeline; Vossough, Arastoo; Sanders, Stephan J; Banka, Siddharth; Findlay, Gregory M; MacArthur, Daniel G; Simons, Cas; Whiffin, Nicola

De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders

剪接因子基因SF3B1的新生变异与神经发育障碍相关。

Uguen, Kevin; Bergot, Tiffany; Scott-Boyer, Marie-Pier; Chapalain, Solène; Desdouets, Camille; Commet, Séverine; Zhu, Changlian; Xu, Yiran; Wang, Yangong; Roscioli, Tony; Tran-Mau-Them, Frederic; Faivre, Laurence; Maraval, Julien; Delanne, Julian; Denommé-Pichon, Anne-Sophie; Vitobello, Antonio; Jost, Céline; Planes, Marc; Hiatt, Susan; Wheeler, Patricia; Gonzaga-Jauregui, Claudia; Wang, Heng; Xin, Baozhong; Sency, Valerie; Kruer, Michael C; Bakhtiari, Somayeh; Sulem, Patrick; Curry, Cynthia; Prescott, Trine; Strobl-Wildemann, Gertrud; Brunet, Theresa; Doco Fenzy, Martine; Courtin, Thomas; Poirsier, Céline; Bjørg Hammer, Trine; Fenger, Christina D; MacPherson, Melissa; Izumi, Kosuke; Leonard, Jacqueline; Li, Dong; Zackai, Elaine H; Glass, Ian A; Ward, Scott; Campeau, Philippe M; Borroto, Maria Carla Hermida; Le Moigno, Laurence; Van Esch, Hilde; De Waele, Liesbeth; Calame, Daniel G; Lupski, James R; Barcia, Giulia; Peduto, Cristina; Planté-Bordeneuve, Pauline; Dupuis, Lucie; Mendoza-Londono, Roberto; Stavropoulos, Dimitri J; Gillibert-Duplantier, Jennifer; Besnard, Thomas; Do Souto Ferreira, Laura; Cogné, Benjamin; Bézieau, Stéphane; Droit, Arnaud; Corcos, Laurent; Lippert, Eric; Férec, Claude; Küry, Sebastien; Bernard, Delphine G

Missense variants in DPYSL5 associated with neurodevelopmental disorders and brain malformations cause impaired neuronal maturation in vitro

DPYSL5基因中的错义变异与神经发育障碍和脑畸形相关,会导致体外神经元成熟受损。

Desprez, Florence; Remize, Solène; François-Moutal, Liberty; Ung, Dévina C; Dangoumau, Audrey; Marouillat, Sylviane; Kennedy, Joanna; Low, Karen J; Kumps, Camille; Unger, Sheila; Keren, Boris; de Sainte Agathe, Jean-Madeleine; Poirsier, Céline; Mirzaa, Ghayda M; Aldinger, Kimberly A; Lesca, Gaetan; Ruault, Valentin; Finnila, Candice R; Kelley, Whitley V; Latner, Donald R; Guptha, Sushma N; Tuttle, Annabelle; Glass, Ian; Chung, Wendy K; Hayek, Jennifer Cassady; Boute, Odile; Moutal, Aubin; Jeanne, Médéric; Laumonnier, Frédéric

DIO3 coordinates photoreceptor development timing and fate stability in human retinal organoids

DIO3 协调人类视网膜类器官中感光细胞的发育时间和命运稳定性

McNerney, Christina; Santiago, Clayton P; Eldred, Kiara C; Glass, Ian; Reh, Tom A; Hernandez, Arturo; Blackshaw, Seth; Lord, Nathan D; Johnston, Robert J Jr

Spatial transcriptomics of developing human lungs defines cellular phenotypes associated with age, lineage and location

对发育中人类肺部的空间转录组学分析揭示了与年龄、谱系和位置相关的细胞表型

Ren, Yue; Danopoulos, Soula; Deutsch, Gail H; Glass, Ian A; Mariani, Thomas J; Bhattacharya, Soumyaroop

Deciding whether to donate fetal tissue for research

决定是否捐献胎儿组织用于研究

MacDuffie, Katherine E; Dempsey, Jennifer C; Cort, Lucinda A; Doherty, Dan; Glass, Ian; Benson, Lyndsey

The impact of delayed evacuation on the quality of human fetal tissue

延迟清宫对人类胎儿组织质量的影响

Otaibi, Yasmeen; Lee, Kevin; Cort, Lucinda; O'Day, Diana R; Dempsey, Jennifer C; Phelps, Ian G; Micks, Elizabeth; Benson, Lyndsey S; Deng, Mei; Doherty, Dan; Prager, Sarah; Glass, Ian A; Aldinger, Kimberly A

Membrane Tension Integrates Physical and Signaling Cues to Gate Cell Fate Transitions

膜张力整合物理和信号线索以控制细胞命运转变

Ali, Gibran; Gibbard, Daniel; Ghelfi, Elisa; Olson, Aaron; Cai, Junming; Balagtas, Aidan; Klein, Isaiah; Maccoux, Emily; Han, Yulong; Miura, Akihiro; Guo, Ming; Glass, Ian; Mori, Munemasa; Brownfield, Douglas G

The evolution of hominin bipedalism in two steps

人科动物双足行走的演化分为两个阶段

Senevirathne, Gayani; Fernandopulle, Serena C; Richard, Daniel; Baumgart, Stephanie L; Christensen, Anika Liv; Fabbri, Matteo; Höppner, Jakob; Jüppner, Harald; Li, Peishu; Bothe, Vivien; Fröbisch, Nadia; Simcock, Ian; Arthurs, Owen J; Calder, Alistair; Freilich, Naomi; Nowlan, Niamh C; Glass, Ian A; Craft, April; Capellini, Terence D